Dimethyl Disulfide → HCID 20285731, compound

HRID 127776Notes

Reaction equation

HRID 127776 reaction equation
Br[C:2]1[S:3][C:4]([CH3:9])=[C:5]([Br:8])[C:6]=1[CH3:7].C([Li])CCC.[CH3:15][S:16]SC>C(OCC)C>[Br:8][C:5]1[C:6]([CH3:7])=[C:2]([S:16][CH3:15])[S:3][C:4]=1[CH3:9]

Participants

5

Conditions

Temperature
-70 °C

Procedure

20.0 G. of 2,4-dibromo-3,5-dimethylthiophene was dissolved in 300 ml. of anhydrous ethyl ether. The resulting solution was cooled to -70° C. with stirring under argon. 32 Ml. of a 2.4 M solution of n-butyl lithium was added slowly and the solution was warmed to -32° C. for 10 minutes and then cooled again to -70° C. 7.5 G. of dimethyl disulfide was added slowly while the temperature was maintained at -70° C. The resulting solution was warmed to room temperature and stirred for 2 hours then poured into ice water, stirred for 15 minutes, and extracted with ethyl ether. The combined ether extracts were washed with water, 5% sodium carbonate, and saturated sodium chloride solution; dried over sodium sulfate, filtered and evaporated to yield 3-bromo-2,4-dimethyl-5-(methylthio)thiophene.

Workup

  1. temperaturethe solution was warmed to -32° C. for 10 minutes
  2. temperaturecooled again to -70° C
  3. temperaturewas maintained at -70° C
  4. temperatureThe resulting solution was warmed to room temperature
  5. stirringstirred for 2 hours
  6. stirringstirred for 15 minutes
  7. extractionextracted with ethyl ether
  8. washThe combined ether extracts were washed with water, 5% sodium carbonate, and saturated sodium chloride solution
  9. dry with materialdried over sodium sulfate
  10. filtrationfiltered
  11. customevaporated

Sources & evidence

ORD record
ord-a5127dd0811844be912a1e2c8c205bdd
Source dataset
uspto-grants-1981_03
Patent number
US04256878

Reaction notes

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